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Propionic anhydride

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This is an old revision of this page, as edited by Emeldir (talk | contribs) at 00:53, 12 September 2016 (preferred IUPAC name (PIN) according to ''Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book)''). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Propanoic anhydride
Names
Preferred IUPAC name
Propanoic anhydride
Other names
Propionic anhydride
Propanoyl propanoate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.004.218 Edit this at Wikidata
RTECS number
  • UF9100000
  • InChI=1S/C6H10O3/c1-3-5(7)9-6(8)4-2/h3-4H2,1-2H3 ☒N
    Key: WYVAMUWZEOHJOQ-UHFFFAOYSA-N ☒N
  • InChI=1/C6H10O3/c1-3-5(7)9-6(8)4-2/h3-4H2,1-2H3
    Key: WYVAMUWZEOHJOQ-UHFFFAOYAJ
  • CCC(=O)OC(=O)CC
Properties
C6H10O3
Molar mass 130.14 g/mol
Appearance Clear liquid, with a strong smell similar to vinegar
Density 1.015 g/cm3, liquid
Melting point −42 °C (−44 °F; 231 K)
Boiling point 167 to 170 °C (333 to 338 °F; 440 to 443 K)
Reacts to give propanoic acid
Viscosity 1.144 cP at ?°C
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
flammable
Flash point 63 °C (145 °F; 336 K)
Safety data sheet (SDS) External MSDS
Related compounds
Related compounds
Acetic anhydride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Propanoic anhydride is an organic compound with the formula (CH3CH2CO)2O. This simple acid anhydride is a colourless liquid. It is a widely used reagent in organic synthesis.

Synthesis

Propanoic anhydride has been prepared by dehydration of propanoic acid using ketene:[1]

2 CH3CH2CO2H + CH2=C=O → (CH3CH2CO)2O + CH3CO2H

Safety

Propanoic anhydride is strong smelling and corrosive, and will cause burns on contact with skin. Vapour can burn eyes and lungs.

Due to its potential use as a precursor in the synthesis of fentanyl and fentanyl analogs, propanoic anhydride is regulated by the United States Drug Enforcement Administration as a List I chemical under the Controlled Substances Act.[2]

References

  1. ^ Williams, J. W. Krynitsky, J. A. (1955). "n-Caproic Anhydride". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 3.
  2. ^ Drugs of Abuse Publication, Chapter 2